Applicants must have

8+ years medical device industry experience in at least one of the following areas:

  • Regulatory
  • Quality
  • Product Development
  • Business Development
  • Marketing
  • FDA Remediation
  • ISO Remediation
  • Medical
  • Preclinical
  • Clinical Trials
  • Reimbursement
  • Executive Management
  • Privacy and Security (HIPAA/HITECH)

Held a Senior, Principal, Director, VP, or Chief level role (or equivalent)

FDA, CE Mark, 21 CFR 820, and/or ISO 13485 experience

Experience in developing and executing strategy in your respective role

Great communication skills - oral and written

If you do not meet these requirements, please do not apply at this time.


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